Canonical Allele Identifier: CA29992577
Gene:

Linked Data

ClinVar Variation Id: 1286950
ClinVar RCV Id: RCV001708575
dbSNP Id: rs72692814
gnomAD v2: 1-149900264-G-C
gnomAD v3: 1-149928372-G-C
gnomAD v4: 1-149928372-G-C
MyVariant Identifiers: chr1:g.149900264G>C (hg19) chr1:g.149928372G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928372G>C , CM000663.2:g.149928372G>C GRCh38
NC_000001.10:g.149900264G>C , CM000663.1:g.149900264G>C GRCh37
NC_000001.9:g.148166888G>C NCBI36
NG_032777.1:g.4881C>G
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